- AbbVie (Irvine, CA)
- …and AbbVie study staff. + Responsible for understanding and addressing applicable regulatory requirements related to the clinical studies, clinician reported ... interpretation, presentation and reporting of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers, regulatory… more
- Astellas Pharma (Northbrook, IL)
- …safety, Toxicology (early phase programs) regulatory , biostatistics, medical affairs , Health Economics, commercial perspectives into clinical development ... voice regarding the potential for impact on planned clinical , medical affairs and commercial strategies. +...meetings, and interactions with opinion leaders. Serves as the clinical interface in regulatory authority interactions. +… more
- Vanderbilt University Medical Center (Nashville, TN)
- …education, and research. **Organization:** Quality Admin **Job Summary:** The Associate Director supervises, coordinates and monitors the work activity of a unit ... Quality Administration Laboratory Department is in need of a **Associate Director ** to join the team! **Department Summary:** Our new 110,000-square-foot diagnostic… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Executive Medical Director , Hematology, will provide overall clinical scientific leadership for the C5 program and have responsibility for our clinical ... demonstrates outstanding clinical scientific knowledge applicable to hematology clinical research. The Executive Medical Director , Hematology reports… more
- Bayer (Cambridge, MA)
- …(GCL), with input from and consensus with groups such as Research, Early Development, Regulatory Affairs , and commercial functions; + Serve as an internal expert ... and diverse minds to make a real difference, there's only one choice.** ** Director , Early Clinical Leader - Cardiovascular and Kidney** The Director , Early … more
- Amgen (Washington, DC)
- …team. Join us and transform the lives of patients while transforming your career. Clinical Research Medical Director , Uplizna **What you will do** Let's do this. ... input into the development program(s) + Participate and provide clinical input into safety and regulatory interactions....content input to materials to be used in Scientific Affairs as well as the Commercial Organization + Approximate… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Role Overview** The Sr. Director , Clinical Development is an experienced clinical trialist who will ... development programs both externally and internally (eg, Medical Affairs , Commercial, CROs, etc.). They will provide clinical... trial data + Supports authorship and review of clinical / regulatory documents (eg, protocols, Investigator… more
- Lilly (IN)
- …and through influence on the compound team that reports through MDU or Medical Affairs . The Director GI Portfolio and Pipeline will facilitate planning and ... the global team (including alliances). Be aware of and ensure that all medical affairs activities are in compliance with Good Clinical Practices (GCPs), company… more
- Elevance Health (Cincinnati, OH)
- ** Clinical Compliance Medical Director ** _Please note that per our policy t_ _his role enables associates to work virtually full-time, with the exception of ... for employment, unless an accommodation is granted as required by law._ The ** Clinical Compliance Medical Director ** is responsible for providing clinical … more
- Takeda Pharmaceuticals (Boston, MA)
- …will inspire you and empower you to shine? Join us as a Executive Medical Director , Oncology Clinical Sciences in our Cambridge office. At Takeda, we are ... Development Plan (IGDP). Responsible for review of synopses, other relevant clinical study documents and Critical Study Results. Provide leadership and oversight… more